Braemar, Inc.
FDA 510(k) & PMA Approved Devices — 5 products
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Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K081444 | BRAEMAR FUSION WIRELESS - AMBULATORY ECG ARRHYTHMIA MONITORING SYSTEM | DSI | 2008-07-31 | View |
| 510(k) | K072008 | BRAEMAR ER900 WIRELESS SERIES ARRHYTHMIA EVENT RECORDER | DRG | 2007-10-03 | View |
| 510(k) | K071733 | DL900 SERIES HOLTER RECORDER | MWJ | 2007-07-24 | View |
| 510(k) | K071011 | MODIFICATION TO: BRAEMAR ER900 SERIES ENHANCED ALGORITHM ECG EVENT RECORDER | MWJ | 2007-04-27 | View |
| 510(k) | K042469 | BRAEMAR ER800 SERIES ENHANCED ALGORITHM EVENT RECORDER | MWJ | 2004-10-06 | View |
No matching devices.
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